Staron Jakub, Boron Bożena, Karcz Dariusz, Szczygieł Małgorzata, Fiedor Leszek
Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Krakow, Poland.
Curr Med Chem. 2015;22(26):3054-74. doi: 10.2174/0929867322666150818104034.
Since photodynamic therapy emerged as a promising cancer treatment, the development of photosensitizers has gained great interest. In this context, the photosynthetic pigments, chlorophylls and bacteriochlorophylls, as excellent natural photosensitizers, attracted much attention. In effect, several (bacterio) chlorophyll-based phototherapeutic agents have been developed and (or are about to) enter the clinics. The aim of this review article is to give a survey of the advances in the synthetic chemistry of these pigments which have been made over the last decade, and which are pertinent to the application of their derivatives as photosensitizers for photodynamic therapy (PDT). The review focuses on the synthetic strategies undertaken to obtain novel derivatives of (bacterio)chlorophylls with both enhanced photosensitizing and tumorlocalizing properties, and also improved photo- and chemical stability. These include modifications of the C- 17-ester moiety, the isocyclic ring, the central binding pocket, and the derivatization of peripheral functionalities at the C-3 and C-7 positions with carbohydrate-, peptide-, and nanoparticle moieties or other residues. The effects of these modifications on essential features of the pigments are discussed, such as the efficiency of reactive oxygen species generation, photostability, phototoxicity and interactions with living organisms. The review is divided into several sections. In the first part, the principles of PDT and photosensitizer action are briefly described. Then the relevant photophysical features of (bacterio)chlorophylls and earlier approaches to their modification are summarized. Next, a more detailed overview of the progress in synthetic methods is given, followed by a discussion of the effects of these modifications on the photophysics of the pigments and on their biological activity.
自从光动力疗法成为一种有前景的癌症治疗方法以来,光敏剂的开发引起了极大的兴趣。在此背景下,光合色素,叶绿素和细菌叶绿素,作为出色的天然光敏剂,备受关注。实际上,几种基于(细菌)叶绿素的光治疗剂已经开发出来并(或即将)进入临床。这篇综述文章的目的是概述这些色素在过去十年中合成化学方面的进展,这些进展与它们的衍生物作为光动力疗法(PDT)光敏剂的应用相关。综述重点关注为获得具有增强的光敏和肿瘤定位特性以及改善的光稳定性和化学稳定性的(细菌)叶绿素新型衍生物所采用的合成策略。这些策略包括对C-17-酯部分、异环、中心结合口袋的修饰,以及在C-3和C-7位置用碳水化合物、肽和纳米颗粒部分或其他残基对外围官能团进行衍生化。讨论了这些修饰对色素基本特性的影响,如活性氧生成效率、光稳定性、光毒性以及与生物体的相互作用。综述分为几个部分。在第一部分,简要描述了光动力疗法和光敏剂作用的原理。然后总结了(细菌)叶绿素的相关光物理特性以及早期对其进行修饰的方法。接下来,对合成方法的进展进行了更详细的概述,随后讨论了这些修饰对色素光物理性质及其生物活性的影响。